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Spectra Optia Apheresis System (2019-07-19)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2019/70635r-eng.php

Aug 7, 2019 ... the return pump still rotating in the direction of patient were being triggered without cause. Root cause investigation shows the issue being related to the current pump driver CCA (777200-544) that was implemented with Gen 2 e-box. Affected products Spectra Optia Apheresis System Lot or serial number 1P02482 1P06123 1P06193 Model or catalog number 61000 Companies

Auum Omega 3D Softgels (January 02, 2013)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2013/16867r-eng.php

Mar 1, 2015 ... of age Depth of distribution Product is distributed to direct accounts (clinics, practitioners) in Ontario. Affected products Auum Omega 3D Softgels DIN, NPN, DIN-HIM NPN 80020633 Dosage form Softgel Strength 2500 mg Seal Oil 3.125 mcg (125 IU) Vitamin D3 Lot or serial number 12071 Companies Recalling Firm Auum Inc. PO Box 898 Iroquois Falls ON Ontario Canada P0K

Auum Omega 3 Sublingual D (January 02, 2013)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2013/16865r-eng.php

Mar 1, 2015 ... of age Depth of distribution Product is distributed to direct accounts (clinics, practitioners) in Ontario. Affected products Auum Omega 3 Sublingual D DIN, NPN, DIN-HIM NPN 80014581 Dosage form Liquid Strength 2500 mg Seal Oil 12.5 mcg (500 IU) Vitamin D3 Lot or serial number J0911, J1241, J2601, 10473, J341, J2851, 11262, 11029, 11532, 12133 Companies Recalling

R2 Microphone for Cox Box, Cox Box Mini, and Megaphone

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2012/15947r-eng.php

Dec 3, 2012 ... (GP) Identification number: RA-15947 Affected products What you should do Affected products R2 Microphone for Cox Box, Cox Box Mini, and Megaphone Product description This recall involves NK R2 microphones manufactured before September 1, 2012. The recalled product is a microphone designed to be used by the navigator (coxswain) of rowed racing boats to direct

Hand Care - Hand Disinfectant (February 04, 2010)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2010/10107r-eng.php

Mar 1, 2015 ..., Healthcare Professionals, Hospitals Identification number: RA-2010A54 Reason Depth of distribution Affected products Reason No market authorization for hand sanitizer and no Drug Establishment Licence. Depth of distribution Distributed nationally to Canadian Norwex consultants (for the purpose of direct home sales) and to USA Norwex Consultants. Affected products

PRIMAXIN 500 (imipenem and cilastatin sodium) for injection - Incorrect Labelling Information

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2016/60102a-eng.php

Sep 6, 2016 ... diluted concentration after reconstitution. It indicates the diluted concentration is 2.5 mg/mL instead of 5 mg/mL (when prepared as per the instructions in the package insert). Referencing this incorrect information could lead to a potential dosing error. Healthcare professionals are directed to consult the package insert or the Canadian Product Monograph

IXIARO Japanese Encephalitis Vaccine (inactivated, adsorbed) - Recall of Lot JEV09L37C - For the Public

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2011/15924a-eng.php

Mar 1, 2013 ... X1A 2L9 Phone: 867-920-8646 Fax: 867-873-0442 Web site: Northwest Territories Dept. of Health and Social Services Nunavut Office of the Chief Medical Health Officer Dept. of Health and Social Services Box 1000, Station 1000 Iqaluit, Nunavut, X0A 0H0 Phone: 867-975-5700 Fax: 867-979-3190 Ontario Direct all forms to your local public health unit. Contact

Shenzhen Wismec Electronics Co., Ltd. recalls Wismec Exo Skeleton Vaporizers

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2018/66530r-eng.php

Apr 19, 2018 ... number ES300, a 7-digit serial number (S/N) prefix ranging from 6046771 to 6212845, UPC code: 6970470011599 and P/N: W084. The serial number prefix appears on the warranty card and the label of the product box. Hazard identified The recalled products have a firmware issue that can lead to a charging failure causing overcurrent to be supplied to the batteries

BiCNU (carmustine for injection) - Type I Recall due to Risk of Infection - Notice to Hospitals

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2009/14593a-eng.php

Mar 6, 2013 ... and segregate any product with the affected lot number and return the affected product according to the directions below. Though the 3 mL ampoules of sterile diluent lot number 8724CA provided with BiCNU are not impacted by this recall event, they must also be returned. Should any recalled product be found, please remove it from inventory and return both the vial

Various Dimension Chemistry, Clinical Chemistry, EXL and XP System Products - IV (2014-10-10)

https://www.healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/2014/42145r-eng.php

... Phosphatase (ALPI) Assay Affected products 1) Dimension EXL System - C-Reactive Protein (CRP) Assay Lot or serial number Not applicable Model or catalog number 10444894 DF37 Companies Manufacturer Siemens Healthcare Diagnostics Inc. 500 GBC Drive, Mailstop 514, PO Box 6101 Newark 19714-6101 Delaware UNITED STATES 2) Dimension EXL System -Direct Bilirubin (DBI) Assay

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